What can causal networks tell us about metabolic pathways?

Graphical models describe the linear correlation structure of data and have been used to establish causal relationships among phenotypes in genetic mapping populations. Data are typically collected at a single point in time. Biological processes on the other hand are often non-linear and display tim...

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Main Authors: Rachael Hageman Blair, Daniel J Kliebenstein, Gary A Churchill
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS Computational Biology
Online Access:http://europepmc.org/articles/PMC3320578?pdf=render
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spelling doaj-61f2f7f573d9418e9369c08a0533be092020-11-25T01:57:43ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582012-01-0184e100245810.1371/journal.pcbi.1002458What can causal networks tell us about metabolic pathways?Rachael Hageman BlairDaniel J KliebensteinGary A ChurchillGraphical models describe the linear correlation structure of data and have been used to establish causal relationships among phenotypes in genetic mapping populations. Data are typically collected at a single point in time. Biological processes on the other hand are often non-linear and display time varying dynamics. The extent to which graphical models can recapitulate the architecture of an underlying biological processes is not well understood. We consider metabolic networks with known stoichiometry to address the fundamental question: "What can causal networks tell us about metabolic pathways?". Using data from an Arabidopsis Bay[Formula: see text]Sha population and simulated data from dynamic models of pathway motifs, we assess our ability to reconstruct metabolic pathways using graphical models. Our results highlight the necessity of non-genetic residual biological variation for reliable inference. Recovery of the ordering within a pathway is possible, but should not be expected. Causal inference is sensitive to subtle patterns in the correlation structure that may be driven by a variety of factors, which may not emphasize the substrate-product relationship. We illustrate the effects of metabolic pathway architecture, epistasis and stochastic variation on correlation structure and graphical model-derived networks. We conclude that graphical models should be interpreted cautiously, especially if the implied causal relationships are to be used in the design of intervention strategies.http://europepmc.org/articles/PMC3320578?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Rachael Hageman Blair
Daniel J Kliebenstein
Gary A Churchill
spellingShingle Rachael Hageman Blair
Daniel J Kliebenstein
Gary A Churchill
What can causal networks tell us about metabolic pathways?
PLoS Computational Biology
author_facet Rachael Hageman Blair
Daniel J Kliebenstein
Gary A Churchill
author_sort Rachael Hageman Blair
title What can causal networks tell us about metabolic pathways?
title_short What can causal networks tell us about metabolic pathways?
title_full What can causal networks tell us about metabolic pathways?
title_fullStr What can causal networks tell us about metabolic pathways?
title_full_unstemmed What can causal networks tell us about metabolic pathways?
title_sort what can causal networks tell us about metabolic pathways?
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2012-01-01
description Graphical models describe the linear correlation structure of data and have been used to establish causal relationships among phenotypes in genetic mapping populations. Data are typically collected at a single point in time. Biological processes on the other hand are often non-linear and display time varying dynamics. The extent to which graphical models can recapitulate the architecture of an underlying biological processes is not well understood. We consider metabolic networks with known stoichiometry to address the fundamental question: "What can causal networks tell us about metabolic pathways?". Using data from an Arabidopsis Bay[Formula: see text]Sha population and simulated data from dynamic models of pathway motifs, we assess our ability to reconstruct metabolic pathways using graphical models. Our results highlight the necessity of non-genetic residual biological variation for reliable inference. Recovery of the ordering within a pathway is possible, but should not be expected. Causal inference is sensitive to subtle patterns in the correlation structure that may be driven by a variety of factors, which may not emphasize the substrate-product relationship. We illustrate the effects of metabolic pathway architecture, epistasis and stochastic variation on correlation structure and graphical model-derived networks. We conclude that graphical models should be interpreted cautiously, especially if the implied causal relationships are to be used in the design of intervention strategies.
url http://europepmc.org/articles/PMC3320578?pdf=render
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